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Analysis of predictors of rapid progression of non-offender vascular TCFA plaques

Analysis of predictors of rapid progression of non-offender vascular TCFA plaques

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500102381
Enrollment
Unknown
Registered
2025-05-14
Start date
2025-05-18
Completion date
Unknown
Last updated
2025-05-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute coronary syndrome

Interventions

Observation group:None

Sponsors

The Second Affiliated Hospital of Harbin Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: General inclusion criteria: 1) age >= 18 years old; 2) AMI onset =2.5mm (visual diameter stenosis: 30%-80%).

Exclusion criteria

Exclusion criteria: General exclusion criteria: 1) cardiogenic shock or refractory hypotension (Killip class IV) 2) Use of intravenous vasopressors at randomization, Patients with intraaortic balloon counterpulsation or other mechanical circulatory support device 3) patients treated with endotracheal intubation 4) patients treated with thrombolysis prior to admission 5) pregnant women with creatinine clearance calculated by the Cockcroft-Gault formula; 7) non-cardiac causes with an expected survival time less than 1 year; 8) The patient was allergic to iodinated contrast media; 9) patients are expected to be unable to receive antiplatelet therapy for at least 6 months; 10) patients with prior bypass surgery or planned coronary artery bypass grafting; 12) other conditions (e.g., dementia, substance abuse including drug use and other causes of drug dependence) that may interfere with follow-up. Angiographic exclusion criteria: 1) unable to detect vessel boundaries or poor filling of contrast medium, unable to see the branch opening lesions in multi-position coronary angiography, or excessive overlap of stenosis segments or severe distortion of target vessels. 2) coronary artery disease requiring surgical bypass grafting; 3) inability to identify infarct-related or non-infarct-related vessels based on the available evidence.

Design outcomes

Primary

MeasureTime frame
Fiber cap thickness;

Countries

China

Contacts

Public ContactHuai Yu

The Second Affiliated Hospital of Harbin Medical University

yuhuai1111@163.com+86 138 4511 3852

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026